FDA Inspection 679456 — LGM Pharma Solutions, LLC.

LGM Pharma Solutions, LLC. — FEI 3017140511

The FDA completed an inspection of LGM Pharma Solutions, LLC. on Sep 8, 2010 in Rosenberg, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 8, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rosenberg, TX (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
189021 CFR 211.165(e)Test methods
440621 CFR 211.194(a)(2)Suitability of testing methods verified

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.